Effect of Bed Height on Chest Compression Quality and Provider Biomechanics During Pediatric CPR Simulation

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAkdeniz University

About this trial

High-quality chest compressions are critical for outcomes after pediatric cardiac arrest, yet rescuer ergonomics and bed height may adversely affect compression quality and fatigue. This randomized crossover simulation study will evaluate how four different bed-height settings influence pediatric CPR quality and rescuer biomechanics. Pediatric emergency medicine residents will perform 2-minute chest-compression-only CPR on a pediatric manikin placed on a hospital bed under four bed-height conditions in randomized order across separate sessions. CPR quality metrics from the manikin's feedback system, rescuer fatigue, physiologic responses, and arm angle over time will be compared to identify an ergonomically optimal bed-height approach.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Pediatric resident/assistant physician working in the Department of Pediatrics (Akdeniz University) with valid ÇİYAD certification

Willing and able to provide written informed consent

Able to perform a 2-minute continuous chest-compression CPR cycle on a pediatric manikin

Disqualifiers

Known chronic cardiopulmonary disease that may limit physical exertion during CPR

Known musculoskeletal disorder or chronic condition that may affect CPR performance

Acute injury/illness at the time of participation that could impair safe CPR performance

Refusal or inability to provide informed consent

Trial design

Treatments tested in this trial

  • Fixed Standard Bed Height (58 cm)
  • Anthropometry-Based Bed Height (Patella Midpoint)
  • Anthropometry-Based Bed Height (Lower One-Third Patella-ASIS)
  • Self-Selected Bed Height

Treatment groups

25 Participants
are divided into 4 treatment groups

Sponsors and collaborators